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Comparison · NCT01557322-455429be

Etanercept vs nbDMARDs: Number of Participants With Chest X-Ray Prior to New Therapy

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Etanercept vs nbDMARDs: Number of Participants With Chest X-Ray Prior to New Therapy. Trial comparisons, record NCT01557322-455429be. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01557322-455429be

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.9430.9010.968wilson
Risk in group 20.5150.4890.541wilson
Risk difference, group 1 minus group 20.4280.3790.464newcombe hybrid score
Risk ratio, group 1 over group 21.831.721.95log
Odds ratio, group 1 over group 215.78.4529.1log
Number needed to treat, for one more participant with the outcome on Etanercept than on nbDMARDs2.332.152.64from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Etanercept
Participants with moderate rheumatoid arthritis (RA), defined as disease activity score based on 28-joints count (DAS28) more than (\>) 3.2 to less than or equal to (\<=) 5.1, who received etanercept (ETN, as their first biological drug) in doses as per approved product label or summary of product characteristics (SmPC), were followed retrospectively using the data in British Society for Rheumatology Biologics Register (BSRBR) for 5 years. The doses had been adjusted according to medical and therapeutic necessity.
183194OG000
Group 2nbDMARDs
Biological naïve participants with moderate RA, defined as DAS28 \>3.2 to \<=5.1, who received non-biologic disease modifying anti-rheumatic drugs (nbDMARDs) in doses as per approved product label or SmPC, were followed retrospectively using the data in BSRBR for 5 years. The doses had been adjusted according to medical and therapeutic necessity.
7421,441OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Chest X-Ray Prior to New Therapy
Description
Time frame
Baseline
Population
Analysis population included all enrolled participants with moderate RA at baseline. Here N (number of participants analyzed) signifies participants who were evaluable for this measure.

Source ClinicalTrials.gov

Trial

Title
Characterize Patients With Moderately Active Rheumatoid Arthritis (RA)
NCT number
NCT01557322
Phases
Conditions
Rheumatoid Arthritis
Interventions
etanercept, methotrexate (MTX)
Lead sponsor
Pfizer
Results first posted
2013-10-31

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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